BR0312648A - Process for preparing certain pyrrole triazine compounds - Google Patents
Process for preparing certain pyrrole triazine compoundsInfo
- Publication number
- BR0312648A BR0312648A BR0312648-0A BR0312648A BR0312648A BR 0312648 A BR0312648 A BR 0312648A BR 0312648 A BR0312648 A BR 0312648A BR 0312648 A BR0312648 A BR 0312648A
- Authority
- BR
- Brazil
- Prior art keywords
- compounds
- formula
- preparing certain
- triazine compounds
- useful
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Molecular Biology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Gastroenterology & Hepatology (AREA)
- Vascular Medicine (AREA)
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- Obesity (AREA)
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Abstract
"PROCESSO PARA PREPARAçãO DE COMPOSTOS PIRROLO TRIAZINA, COMPOSIçãO E USO DOS MESMOS". A presente invenção refere-se a um processo para preparação de certos compostos pirroltriazina da fórmula (I) e seus sais farmaceuticamente aceitáveis. Os compostos de fórmula (I) inibem a atividade tirosina cinase de receptores de fator de crescimento tais como VEGFR-2 e FGFR-1, pelo que tornando-os úteis como agentes anticâncer. Os compostos de fórmula I também são úteis para o tratamento de outras doenças associadas com caminhos de transdução de sinal operando através de receptores de fator de crescimento."PROCESS FOR PREPARATION OF TRIAZINE PIRROLO COMPOUNDS, COMPOSITION AND USE OF THE SAME". The present invention relates to a process for preparing certain pyrroltriazine compounds of formula (I) and their pharmaceutically acceptable salts. The compounds of formula (I) inhibit the growth factor receptor tyrosine kinase activity such as VEGFR-2 and FGFR-1, making them useful as anticancer agents. The compounds of formula I are also useful for treating other diseases associated with signal transduction pathways operating through growth factor receptors.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39725602P | 2002-07-19 | 2002-07-19 | |
US44721303P | 2003-02-13 | 2003-02-13 | |
US10/622,280 US6933386B2 (en) | 2002-07-19 | 2003-07-18 | Process for preparing certain pyrrolotriazine compounds |
PCT/US2003/022755 WO2004009542A2 (en) | 2002-07-19 | 2003-07-21 | Process for preparing certain pyrrolotriazine compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0312648A true BR0312648A (en) | 2005-08-02 |
Family
ID=30773518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0312648-0A BR0312648A (en) | 2002-07-19 | 2003-07-21 | Process for preparing certain pyrrole triazine compounds |
Country Status (12)
Country | Link |
---|---|
US (1) | US6933386B2 (en) |
EP (1) | EP1554281A4 (en) |
JP (1) | JP2006502120A (en) |
CN (1) | CN1665817A (en) |
AU (1) | AU2003256645A1 (en) |
BR (1) | BR0312648A (en) |
CA (1) | CA2492861A1 (en) |
IL (1) | IL165985A0 (en) |
MX (1) | MXPA05000344A (en) |
PL (1) | PL375316A1 (en) |
TW (1) | TWI272271B (en) |
WO (1) | WO2004009542A2 (en) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6867300B2 (en) * | 2000-11-17 | 2005-03-15 | Bristol-Myers Squibb Company | Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors |
WO2003090912A1 (en) * | 2002-04-23 | 2003-11-06 | Bristol-Myers Squibb Company | Pyrrolo-triazine aniline compounds useful as kinase inhibitors |
WO2003091229A1 (en) | 2002-04-23 | 2003-11-06 | Bristol-Myers Squibb Company | Aryl ketone pyrrolo-triazine compounds useful as kinase inhibitors |
TWI329112B (en) * | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
PL378121A1 (en) | 2003-02-05 | 2006-03-06 | Bristol-Myers Squibb Company | Process for preparing pyrrolotriazine kinase inhibitors |
US7102001B2 (en) * | 2003-12-12 | 2006-09-05 | Bristol-Myers Squibb Company | Process for preparing pyrrolotriazine |
US20060014741A1 (en) * | 2003-12-12 | 2006-01-19 | Dimarco John D | Synthetic process, and crystalline forms of a pyrrolotriazine compound |
US7064203B2 (en) | 2003-12-29 | 2006-06-20 | Bristol Myers Squibb Company | Di-substituted pyrrolotriazine compounds |
MY145634A (en) * | 2003-12-29 | 2012-03-15 | Bristol Myers Squibb Co | Pyrrolotriazine compounds as kinase inhibitors |
US7102002B2 (en) * | 2004-06-16 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7173031B2 (en) * | 2004-06-28 | 2007-02-06 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7432373B2 (en) * | 2004-06-28 | 2008-10-07 | Bristol-Meyers Squibb Company | Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors |
TW200600513A (en) * | 2004-06-30 | 2006-01-01 | Bristol Myers Squibb Co | A method for preparing pyrrolotriazine compounds |
US7253167B2 (en) * | 2004-06-30 | 2007-08-07 | Bristol-Myers Squibb Company | Tricyclic-heteroaryl compounds useful as kinase inhibitors |
US7102003B2 (en) * | 2004-07-01 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
US7419972B2 (en) * | 2004-07-02 | 2008-09-02 | Schering Ag | 2-substituted estra-1,3,5(10)-trien-17-ones as inhibitors of 17β-hydroxy steroid dehydrogenase type 1 |
US7504521B2 (en) * | 2004-08-05 | 2009-03-17 | Bristol-Myers Squibb Co. | Methods for the preparation of pyrrolotriazine compounds |
TW200618803A (en) | 2004-08-12 | 2006-06-16 | Bristol Myers Squibb Co | Process for preparing pyrrolotriazine aniline compounds useful as kinase inhibitors |
US7151176B2 (en) * | 2004-10-21 | 2006-12-19 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
US7514435B2 (en) * | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
PE20070855A1 (en) | 2005-12-02 | 2007-10-14 | Bayer Pharmaceuticals Corp | DERIVATIVES OF 4-AMINO-PYRROLOTRIAZINE SUBSTITUTE AS KINASE INHIBITORS |
KR20130141706A (en) | 2005-12-02 | 2013-12-26 | 바이엘 헬스케어 엘엘씨 | Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
US8063208B2 (en) | 2006-02-16 | 2011-11-22 | Bristol-Myers Squibb Company | Crystalline forms of (3R,4R)-4-amino-1-[[4-[(3-methoxyphenyl)amino]pyrrolo[2,1-f][1,2,4]triazin-5-yl]methyl]piperidin-3-ol |
PT2010538E (en) * | 2006-04-21 | 2013-02-22 | Bristol Myers Squibb Co | Process for the preparation of ý(1r), 2s¨-2-aminopropionic acid 2-ý4-(4-fluoro-2-methyl-1h-indol-5-yloxy)-5-methylpyrroloý2,1-f¨ý1,2,4¨triazin-6-yloxy¨-1-methylethyl ester |
ATE537450T1 (en) | 2006-06-30 | 2011-12-15 | Schering Corp | IGFBP2 BIOMARKERS |
CL2007003158A1 (en) | 2006-11-02 | 2008-05-16 | Astrazeneca Ab | PROCEDURE FOR PREPARATION OF COMPOUNDS DERIVED FROM QUINAZOLINA OR ITS PHARMACEUTICALLY ACCEPTABLE SALTS; INTERMEDIARY COMPOUNDS; PREPARATION PROCEDURE |
KR101502634B1 (en) | 2007-02-08 | 2015-03-16 | 코덱시스, 인코포레이티드 | Ketoreductases and uses thereof |
CA2702637A1 (en) | 2007-10-22 | 2009-04-30 | Schering Corporation | Fully human anti-vegf antibodies and methods of using |
ES2539620T3 (en) | 2008-12-19 | 2015-07-02 | Cephalon, Inc. | Pyrrolotriazine as an inhibitor of ALK and JAK2 |
US8691981B2 (en) * | 2010-02-03 | 2014-04-08 | Bristol-Myers Squibb Company | Crystalline forms of (S)-1-(4-(5-cyclopropyl-1H-pyrazol-3-ylamino)pyrrolo[1,2-f][1,2,4]triazin-2-yl)-N-(6-fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide |
CN102603718B (en) * | 2012-02-08 | 2014-01-29 | 武汉凯斯瑞科技有限公司 | Synthesis method of cediranib |
CN103420892A (en) * | 2012-05-18 | 2013-12-04 | 苏州爱斯鹏药物研发有限责任公司 | Preparation method of 4-fluoroindole |
CN104955459B (en) | 2012-11-05 | 2019-02-01 | 南特知识产权控股有限责任公司 | Substituted indoles -5- amphyl and its treatment use |
CN107954991A (en) | 2013-03-15 | 2018-04-24 | 南特生物科学公司 | Substituted indoles -5- amphyls and their treatment use |
WO2015081783A1 (en) * | 2013-12-06 | 2015-06-11 | 江苏奥赛康药业股份有限公司 | Pyrrolo[2,1-f][1,2,4]triazine derivative, and preparation method and use thereof |
US9388239B2 (en) | 2014-05-01 | 2016-07-12 | Consejo Nacional De Investigation Cientifica | Anti-human VEGF antibodies with unusually strong binding affinity to human VEGF-A and cross reactivity to human VEGF-B |
CA3038280A1 (en) | 2015-09-30 | 2017-04-06 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. - Generalverwaltung | Heteroaryl derivatives as sepiapterin reductase inhibitors |
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JP4649046B2 (en) | 1999-05-21 | 2011-03-09 | ブリストル−マイヤーズ スクイブ カンパニー | Pyrrotriazine inhibitor of kinase |
NZ523987A (en) * | 2000-08-09 | 2004-10-29 | Astrazeneca Ab | Indole, azaindole and indazole derivatives having VEGF inhibiting activity |
ES2259051T3 (en) | 2000-11-17 | 2006-09-16 | Bristol-Myers Squibb Company | PROCEDURES FOR THE TREATMENT OF DOLENCES ASSOCIATED WITH QUINASE P38 AND PIRROLOTRIACINE COMPOUNDS USED AS QUINASE INHIBITORS. |
US6670357B2 (en) | 2000-11-17 | 2003-12-30 | Bristol-Myers Squibb Company | Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors |
-
2003
- 2003-07-18 TW TW092119890A patent/TWI272271B/en not_active IP Right Cessation
- 2003-07-18 US US10/622,280 patent/US6933386B2/en not_active Expired - Lifetime
- 2003-07-21 CN CN038162016A patent/CN1665817A/en active Pending
- 2003-07-21 AU AU2003256645A patent/AU2003256645A1/en not_active Abandoned
- 2003-07-21 JP JP2004523221A patent/JP2006502120A/en not_active Withdrawn
- 2003-07-21 MX MXPA05000344A patent/MXPA05000344A/en active IP Right Grant
- 2003-07-21 CA CA002492861A patent/CA2492861A1/en not_active Abandoned
- 2003-07-21 BR BR0312648-0A patent/BR0312648A/en not_active IP Right Cessation
- 2003-07-21 WO PCT/US2003/022755 patent/WO2004009542A2/en active Application Filing
- 2003-07-21 IL IL16598503A patent/IL165985A0/en unknown
- 2003-07-21 EP EP03765846A patent/EP1554281A4/en not_active Withdrawn
- 2003-07-21 PL PL03375316A patent/PL375316A1/en not_active Application Discontinuation
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US20040077858A1 (en) | 2004-04-22 |
JP2006502120A (en) | 2006-01-19 |
EP1554281A4 (en) | 2009-02-25 |
US6933386B2 (en) | 2005-08-23 |
WO2004009542A3 (en) | 2004-05-13 |
IL165985A0 (en) | 2006-01-15 |
TW200409776A (en) | 2004-06-16 |
PL375316A1 (en) | 2005-11-28 |
EP1554281A2 (en) | 2005-07-20 |
WO2004009542A2 (en) | 2004-01-29 |
AU2003256645A1 (en) | 2004-02-09 |
CA2492861A1 (en) | 2004-01-29 |
TWI272271B (en) | 2007-02-01 |
CN1665817A (en) | 2005-09-07 |
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